STERILE TUBULAR UNBLEACHED STOCKINETTE
FDA 510(k) clearance K760750 · decided 1976-10-08
Clearance details
- K-number
- K760750
- Device name
- STERILE TUBULAR UNBLEACHED STOCKINETTE
- Applicant
- Dennison Manufacturing Co.
- Decision
- Substantially Equivalent
- Date received
- 1976-10-01
- Decision date
- 1976-10-08
- Days to decision
- 7 days
- Clearance type
- Traditional
- Product code
- JLG
- Device class
- 1
- Regulation number
- 862.1290
- Medical specialty
- Clinical Chemistry
- Advisory committee
- Clinical Chemistry
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| WAKO NEFA C TEST (K812081) | Wako Chemicals USA, Inc. | 1981-08-12 |
Recalls involving this device
No recalls on record reference this clearance.